Variant report

Variant	rs1584760
Chromosome Location	chr1:215223052-215223053
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs10494989	0.88[ASN][1000 genomes]
rs10494991	0.95[ASN][1000 genomes]
rs10494992	0.95[ASN][1000 genomes]
rs10779633	0.89[ASN][1000 genomes]
rs10779634	0.88[ASN][1000 genomes]
rs10779635	0.92[ASN][1000 genomes]
rs12026832	0.92[ASN][1000 genomes]
rs12141327	0.91[ASN][1000 genomes]
rs1377173	0.89[ASN][1000 genomes]
rs1377175	0.92[ASN][1000 genomes]
rs1377177	0.95[ASN][1000 genomes]
rs1452608	0.89[ASN][1000 genomes]
rs1452609	0.89[ASN][1000 genomes]
rs1452610	0.89[ASN][1000 genomes]
rs1452620	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1584759	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1597847	0.85[ASN][1000 genomes]
rs17024148	0.85[ASN][1000 genomes]
rs2123331	0.85[ASN][1000 genomes]
rs2262937	0.89[ASN][1000 genomes]
rs2601607	0.89[ASN][1000 genomes]
rs2601609	0.85[ASN][1000 genomes]
rs2601610	0.89[ASN][1000 genomes]
rs2601611	0.89[ASN][1000 genomes]
rs2601612	0.89[ASN][1000 genomes]
rs2601613	0.88[ASN][1000 genomes]
rs2601614	0.89[ASN][1000 genomes]
rs2601615	0.89[ASN][1000 genomes]
rs2601616	0.89[ASN][1000 genomes]
rs2601617	0.88[ASN][1000 genomes]
rs2601618	0.89[ASN][1000 genomes]
rs2601619	0.88[ASN][1000 genomes]
rs2601620	0.89[ASN][1000 genomes]
rs2601621	0.88[ASN][1000 genomes]
rs2601622	0.89[ASN][1000 genomes]
rs2601623	0.89[ASN][1000 genomes]
rs2601624	0.89[ASN][1000 genomes]
rs2601625	0.92[ASN][1000 genomes]
rs2601636	0.89[ASN][1000 genomes]
rs2601638	0.89[ASN][1000 genomes]
rs2601639	0.89[ASN][1000 genomes]
rs2601640	0.89[ASN][1000 genomes]
rs2601641	0.89[ASN][1000 genomes]
rs2601646	0.89[ASN][1000 genomes]
rs2601650	0.81[ASN][1000 genomes]
rs2802642	0.89[ASN][1000 genomes]
rs2802643	0.89[ASN][1000 genomes]
rs2802644	0.89[ASN][1000 genomes]
rs2802649	0.89[ASN][1000 genomes]
rs2802650	0.89[ASN][1000 genomes]
rs2802651	0.89[ASN][1000 genomes]
rs2802657	0.94[ASN][1000 genomes]
rs2841574	0.94[ASN][1000 genomes]
rs2841575	0.93[ASN][1000 genomes]
rs2841577	0.93[ASN][1000 genomes]
rs2841581	0.93[ASN][1000 genomes]
rs2841587	0.93[ASN][1000 genomes]
rs2841591	0.92[ASN][1000 genomes]
rs2841592	0.92[ASN][1000 genomes]
rs2841595	0.90[ASN][1000 genomes]
rs2841596	0.89[ASN][1000 genomes]
rs2841597	0.89[ASN][1000 genomes]
rs2841598	0.89[ASN][1000 genomes]
rs2841599	0.89[ASN][1000 genomes]
rs2841600	0.89[ASN][1000 genomes]
rs2841601	0.89[ASN][1000 genomes]
rs2841602	0.89[ASN][1000 genomes]
rs2841604	0.89[ASN][1000 genomes]
rs2841605	0.89[ASN][1000 genomes]
rs2841606	0.89[ASN][1000 genomes]
rs2841607	0.89[ASN][1000 genomes]
rs2841608	0.89[ASN][1000 genomes]
rs2841609	0.89[ASN][1000 genomes]
rs2841610	0.89[ASN][1000 genomes]
rs2841611	0.83[ASN][1000 genomes]
rs2841612	0.89[ASN][1000 genomes]
rs2841613	0.89[ASN][1000 genomes]
rs2841615	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2841616	0.80[ASN][1000 genomes]
rs4294386	0.89[ASN][1000 genomes]
rs4339836	0.89[ASN][1000 genomes]
rs4348692	0.89[ASN][1000 genomes]
rs4356023	0.89[ASN][1000 genomes]
rs61820010	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv468105	chr1:215167236-215248417	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv549182	chr1:215167236-215248417	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215220200-215225400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr1:215220600-215225000	Weak transcription	NHDF-Ad	bronchial
3	chr1:215221200-215227600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr1:215222400-215224000	Weak transcription	Osteobl	bone
5	chr1:215222800-215242200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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